Shu Zhong

Surface transfer doping induced effective modulation on ambipolar characteristics of few-layer black phosphorus

Black phosphorus, a fast emerging two-dimensional material, has been configured as field effect transistors, showing a hole-transport-dominated ambipolar characteristic. Here we report an effective modulation on ambipolar characteristics of few-layer black phosphorus transistors through in situ surface functionalization with caesium carbonate (Cs2CO3) and molybdenum trioxide (MoO3), respectively. Cs2CO3 is found to strongly electron dope black phosphorus. The electron mobility of black phosphorus is significantly enhanced to ~27 cm(2) V(-1) s(-1) after 10 nm Cs2CO3 modification, indicating a greatly improved electron-transport behaviour. In contrast, MoO3 decoration demonstrates a giant hole-doping effect. In situ photoelectron spectroscopy characterization reveals significant surface charge transfer occurring at the dopants/black phosphorus interfaces. Moreover, the surface-doped black phosphorus devices exhibit a largely enhanced photodetection behaviour. Our findings coupled with the tunable nature of the surface transfer doping scheme ensure black phosphorus as a promising candidate for further complementary logic electronics.

Epitaxial Growth of Single Layer Blue Phosphorus: A New Phase of Two-Dimensional Phosphorus

Blue phosphorus, a previously unknown phase of phosphorus, has been recently predicted by theoretical calculations and shares its layered structure and high stability with black phosphorus, a rapidly rising two-dimensional material. Here, we report a molecular beam epitaxial growth of single layer blue phosphorus on Au(111) by using black phosphorus as precursor, through the combination of in situ low temperature scanning tunneling microscopy and density functional theory calculation. The structure of the as-grown single layer blue phosphorus on Au(111) is explained with a (4 × 4) blue phosphorus unit cell coinciding with a (5 × 5) Au(111) unit cell, and this is verified by the theoretical calculations. The electronic bandgap of single layer blue phosphorus on Au(111) is determined to be 1.10 eV by scanning tunneling spectroscopy measurement. The realization of epitaxial growth of large-scale and high quality atomic-layered blue phosphorus can enable the rapid development of novel electronic and optoelectronic devices based on this emerging two-dimensional material.

Air-Stable Efficient Inverted Polymer Solar Cells Using Solution-Processed Nanocrystalline ZnO Interfacial Layer

In this work, efficient bulk heterojunction (BHJ) organic solar cells (OSC) in inverted configuration have been demonstrated. Power conversion efficiency (PCE) of 3.7% is reported for OSC employing silver top electrodes, molybdenum trioxide (MoO3) as the hole-transport interlayer (HTL), active layer comprising of poly-3-hexylthiophene (P3HT) and [6,6]-phenyl C61 butyric acid methyl ester (PCBM) as well as a nanocrystalline solution-synthesized zinc oxide (ZnO) nanoparticle (NP) film as the electron-transport layer (ETL). By using solution-processable ZnO crystalline NPs as ETL, we can eliminate the typical high temperature processing/annealing step, which is widely adopted in the conventional ZnO ETL fabrication process via the sol-gel method. Such highly crystalline ZnO NP films can enhance charge collection at the electrodes. It is also found that inverted OSCs exhibit greater air stability and lifetime performance compared to the OSC employing the normal structure.

Modulating electronic transport properties of MoS2 field effect transistor by surface overlayers

In situ bottom-gated molybdenum disulfide (MoS2) field effect transistors (FETs) device characterization and in situ ultraviolet photoelectron spectroscopy and x-ray photoelectron spectroscopy measurements were combined to investigate the effect of surface modification layers of C60 and molybdenum trioxide (MoO3) on the electronic properties of single layer MoS2. It is found that C60 decoration keeps MoS2 FET performance intact due to the very weak interfacial interactions, making C60 as an ideal capping layer for MoS2 devices. In contrast, decorating MoO3 on MoS2 induces significant charge transfer at the MoS2/MoO3 interface and largely depletes the electron charge carriers in MoS2 FET devices.

CVD graphene as interfacial layer to engineer the organic donor-acceptor heterojunction interface properties.

We demonstrate the use of chemical-vapor-deposited (CVD) graphene as an effective indium-tin-oxide (ITO) electrode surface modifier to engineer the organic donor-acceptor heterojunction interface properties in an inverted organic solar cell device configuration. As revealed by in situ near-edge X-ray adsorption fine structure measurement, the organic donor-acceptor heterojunction, comprising copper-hexadecafluoro-phthalocyanine (F16CuPc) and copper phthalocyanine (CuPc), undergoes an obvious orientation transition from a standing configuration (molecular π-plane nearly perpendicular to the substrate surface) on the bare ITO electrode to a less standing configuration with the molecular π-plane stacking adopting a large projection along the direction perpendicular to the electrode surface on the CVD graphene-modified ITO electrode. Such templated less-standing configuration of the organic heterojunction could significantly enhance the efficiency of charge transport along the direction perpendicular to the electrode surface in the planar heterojunction-based devices. Compared with the typical standing organic-organic heterojunction on the bare ITO electrode, our in situ ultraviolet photoelectron spectroscopy experiments reveal that the heterojunction on the CVD graphene modified ITO electrode possesses better aligned energy levels with respective electrodes, hence facilitating effective charge collection.

Molecular-scale investigation of C60/p-sexiphenyl organic heterojunction interface.

In situ low-temperature scanning tunneling microscopy (LT-STM) and ultraviolet photoelectron spectroscopy (UPS) experiments have been carried out to investigate the interface properties at the C(60)∕p-sexiphenyl (6P) organic-organic heterojunction interface, including the interfacial energy level alignment and the supramolecular packing structures. As revealed by UPS measurements, the vacuum level is almost aligned at the C(60)∕6P interface, suggesting that the interface is dominated by weak intermolecular interactions, such as van der Waals and π-π interactions. In situ LT-STM experiments also indicate the formation of a molecularly sharp C(60)∕6P interface with hexagonally-close-packed C(60) layers nucleated atop 6P layer on graphite.

Interface investigation of the alcohol-/water-soluble conjugated polymer PFN as cathode interfacial layer in organic solar cells

In this work, in situ ultraviolet photoelectron spectroscopy measurements were used to investigate the working mechanism of an alcohol-/water-soluble conjugated polymer poly [(9,9-bis(3′-(N,N-dimethylamino)propyl)-2,7-fluorene)-alt-2,7-(9,9–dioctylfluorene)] (PFN) as the cathode interfacial layer in organic solar cells from the view of interfacial energy level alignment. Fullerene (C60) was chosen as the model acceptor material in contact with PFN as well as two other cathode interfacial layers ZnO and TiO2 in the configuration of an inverted solar cell structure. Significant charge transfer between PFN modified ITO (indium tin oxide) electrode and C60 is observed due to the low work function of PFN. This results in the Fermi level of the substrate pinned very close to the lowest unoccupied molecular orbital of C60 as well as an additional electric field at the cathode/acceptor interface. Both of them facilitate the electron extraction from the acceptor C60 to the ITO cathode, as confirmed by the electric...

Biopolymer as an electron selective layer for inverted polymer solar cells

In this work, a solution-processable electron selective layer is introduced for inverted polymer solar cells (PSCs). Cationic biopolymer poly(2-(dimethylamino)ethyl methacrylate) (PDMAEMA) is used as a solution-processable work function modifier of indium-tin-oxide transparent conducting electrode to yield efficient inverted PSCs of 3.3% under AM1.5G illumination, with poly(3-hexylthiophene) and [6,6]-phenyl-C61-butyric acid methyl ester as the active layer. Devices using PDMAEMA exhibit greater stability in ambient “working conditions” as compared to devices using ZnO, retaining 90% of peak power conversion efficiency after 8 weeks. Therefore, PDMAEMA has great potential as a universal work function modifier material with high robustness.

Perylene bisimide as the cathode modifier in organic photovoltaics: the role of aggregation morphology on the interlayer performance

Nanorods and nanoparticles of perylene bisimides (PBI-1) were prepared and applied as cathode interlayer in organic photovoltaic devices. The device performance showed an important relationship with the morphology of the interlayer.

A high work function anode interfacial layer via mild temperature thermal decomposition of a C60F36 thin film on ITO

A high work function anode interfacial layer has been developed via a mild temperature thermal decomposition of fluorinated fullerene (C60F36) on ITO at 120 °C. As revealed by in situ ultraviolet photoelectron spectroscopy (UPS) measurements, after the interfacial modification, the ITO electrode work function can be as high as ∼5.62 eV. It also possesses very good air stability even after the exposure to air for more than one day. The thermal annealing induced carbon–fluorine bond breaking was confirmed by in situ X-ray photoelectron spectroscopy (XPS) measurements. The residual F atoms are chemically bonded onto the ITO surface. Taking advantage of such a high work function anode interfacial layer on ITO, enhanced performance of a chloroaluminium phthalocyanine (ClAlPc)/fullerene (C60) planar heterojunction based organic solar cell was observed. The performance enhancement is attributed to the higher anode WF together with the optimal nanoscale morphology, and hence better hole collection efficiency.